Genesⓘ

Dataset:
?Protein-coding genes with reviewed gene-disease associations only.
?Curated and unreviewed gene-disease associations.
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Showing genes starting with "M"
321 to 330 of 893 Genes
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Entrez ID Gene Symbol Gene Name Synonyms Diseases

321
Matrix extracellular phosphoglycoprotein
OF45
Cardiovascular disease, Gout, Hyperuricemia, Osteoarthritis, Osteomalacia, Osteoporosis

322
MER proto-oncogene, tyrosine kinase
MER, RP38, Tyro12, c-Eyk, c-mer
Atrial fibrillation, Retinitis pigmentosa, Carcinoma, Liver cirrhosis, Cone-rod dystrophy, Coronary artery disease, Gout, Hemorrhoid, Iga nephropathy, Metabolic syndrome, Multiple sclerosis, Myocardial infarction, Optic atrophy, Thromboembolism, Thrombosis
View all (1 more)

323
Mesoderm development LRP chaperone
BOCA, MESDC2, OI20
Bone fragility with contractures, arterial rupture, and deafness, Desbuquois syndrome, Osteogenesis imperfecta, Osteoporosis-pseudoglioma syndrome

324
Mesoderm posterior bHLH transcription factor 1
bHLHc5
Congenital heart disease, Myocardial infarction

325
Mesoderm posterior bHLH transcription factor 2
SCDO2, bHLHc6
Spondylocostal dysostosis, Coronary aneurysm, Desbuquois syndrome, Gastroparesis, Jarcho-levin syndrome, Juvenile idiopathic arthritis

326
Mesoderm specific transcript
PEG1
Schizophrenia

327
MET proto-oncogene, receptor tyrosine kinase
AUTS9, DA11, DFNB97, HGFR, RCCP2, c-Met
Distal arthrogryposis, Astrocytoma, Attention deficit hyperactivity disorder, Autism, Isolated sensorineural deafness, Nonsyndromic intellectual disability, Carcinogenesis, Carcinoma, Hepatocellular carcinoma, Non-small-cell lung carcinoma, Renal cell carcinoma, Squamous cell carcinoma, Cognition disorder, Neurodevelopmental disorder, Congenital diaphragmatic hernia
View all (35 more)

328
Methionyl aminopeptidase 1
MAP1A, MetAP1A
Insomnia, Intellectual developmental disorder, Upper aerodigestive tract neoplasm, Uterine fibroid

329
Methionyl aminopeptidase type 1D, mitochondrial
MAP 1D, MAP1D, MetAP 1D, Metap1l
Insomnia, Major depressive disorder, Metabolic syndrome, Schizophrenia, Diabetes mellitus type 2

330
Meteorin, glial cell differentiation regulator
C16orf23, c380A1.2
Ankylosing spondylitis, Atrial fibrillation, Insomnia